HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392091Generated: October 30, 2026
4-Methylmorpholine → HCID 10435474, compound
https://huagongshe.com/reaction/1392091
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoic acid | HCID 12135350 | — |
| Reactant | HCID 58691198 | HCID 58691198 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10435474 | HCID 10435474 | 80.5% |
Reaction Steps
To a solution of (3S,7S)-3-amino-1-(2-methoxyethyl)-7-phenyl-1,3,4,7-tetrahydro-2H-azepin-2-one (6d) (55 mg) in DCM (4 mL) at 0° C. under N2 was added N-[(3,5-difluorophenyl)acetyl]-L-alanine (51 mg), HOBt-hydrate (71 mg), EDAC.HCl (61 mg) and N-methyl morpholine (34 mg). The reaction mixture was stirred 1 h at 0° C. and 3 h at RT, then diluted with 30% hexanes/EtOAc (100 mL). The organic phase was consecutively washed with H2O, 0.2 N HCl, saturated NaHCO3, and brine, dried (Na2SO4), filtered and evaporated. The crude product was purified by flash chromatography (1%-2% MeOH/DCM) to afford a white solid (82 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342007B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-5bbf42c416644fbba99fe8ac96959a53 |
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| Source note | uspto-grants-2008_03 |
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